Manufacturing Visual Inspection

Overview

On Site
$23 - $27
Contract - W2
Contract - 6 month(s)
No Travel Required

Skills

PACKAGING
SOPS
CGMP
VISUAL INSPECTION
BIOTECHNOLOGY

Job Details

Job Description:

Pay Range: $23.80hr - $27.80hr

  • Executes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility.
  • Performs duties under limited supervision and according to standard operating and manufacturing procedures.
  • Executes independently with adequate training, complex fundamental operations as visual inspection, advance visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES Operations and Exceptions.
  • Performs internal support duties including assisting drug product filling and packaging.
  • Executes independently with adequate training fundamental operations:
  • Logistics Coordination
  • Batch record executions
  • Equipment use logs
  • Work order initiation and tracking
  • Support Projects
  • Support Creation/Maintain Training Kits Documents work according to cGMP and cGDP.
  • Adheres to established regulations and follows cGMP established by site.
  • Reports abnormalities and deviations in a timely and accuXX manner.
  • Adheres to safety standards and identifies unsafe situations/habits and escalates appropriately.
  • Maintains production areas according to predefined standards (5s).
  • Maintains own training within compliance and trains other technicians and associates on operations upon completion of the trainer qualification.
  • Contributes to Quality activities such as supporting investigations, corrective actions, and area walk throughs.
Skills:
  • 1 or more years of experience in a cGMP-regulated industry.
  • Strong attention to detail with a "right the first time" mindset.
  • Excellent written and verbal communication skills.
  • Ability to work with computer-based systems and manufacturing execution systems (MES).
  • Capable of reading and understanding SOPs and documenting work according to cGMP standards.
  • Team player with strong collaboration skills.
  • Must be able to read and see clearly.
Education:
  • High school diploma with a minimum of 1 year of work experience in a GMP-regulated industry.
  • Associate's or Bachelor's degree or biotechnology vocational training preferred.
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